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Acetic Acid → tert-Butyl 1-benzyl-6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamate

HRID 2234250
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HRID 2234250 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH2:7][CH:6]([NH:12][C:13](=[O:19])[O:14][C:15]([CH3:18])([CH3:17])[CH3:16])[CH2:5]2.[CH:20](=O)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].CC(O)=O>ClCCCl.CCOC(C)=O>[CH2:20]([N:8]1[C:9]2[C:4](=[CH:3][C:2]([Cl:1])=[CH:11][CH:10]=2)[CH2:5][CH:6]([NH:12][C:13](=[O:19])[O:14][C:15]([CH3:16])([CH3:18])[CH3:17])[CH2:7]1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 240BenzaldehydeHCID 5049666Sodium triacetoxyborohydrideHCID 59297067tert-Butyl 6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamate

생성물 1

HCID 59297049tert-Butyl 1-benzyl-6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamate수율 80%

시약·촉매·용매 2

HCID 11
1,2-Dichloroethane
용매
HCID 8857Ethyl Acetate용매

실험 절차

To a solution of tert-butyl 6-chloro-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (310 mg, 1.096 mmol), prepared as described in Example 19A, in 1,2-dichloroethane (7 mL) was added benzaldehyde (235 mg, 2.193 mmol), followed by sodium triacetoxyborohydride (650 mg, 3.069 mmol) and AcOH (200 mg, 3.29 mmol). The reaction mixture was stirred at RT for 4 h, then diluted with EtOAc, washed with saturated aqueous NaHCO3, water, saturated aqueous NaCl, dried Na2SO4) and concentrated. The resulting residue was chromatographed (silica gel) eluting with EtOAc/hexanes (1:5 ratio) to give the title compound as light yellow foam (325 mg, 80%).

후처리

  1. washwashed with saturated aqueous NaHCO3, water, saturated aqueous NaCl, dried Na2SO4) and
  2. concentrationconcentrated
  3. customThe resulting residue was chromatographed (silica gel)
  4. washeluting with EtOAc/hexanes (1:5 ratio)

출처 및 근거

ORD 기록
ord-48ec7594f5d64d35848421d06afb1c1a
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709647B2

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